{"id":250778,"date":"2021-08-08T15:46:48","date_gmt":"2021-08-08T20:46:48","guid":{"rendered":"https:\/\/www.liveaction.org\/news\/?p=250778"},"modified":"2021-08-07T02:28:59","modified_gmt":"2021-08-07T07:28:59","slug":"determined-mom-medical-breakthrough-down-syndrome","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/determined-mom-medical-breakthrough-down-syndrome\/","title":{"rendered":"Determined mom makes medical breakthrough for children with Down syndrome"},"content":{"rendered":"<div style=\"margin-top: 0px; margin-bottom: 0px;\" class=\"sharethis-inline-share-buttons\" ><\/div><p>A mom of a child with Down syndrome says she was repeatedly ignored by doctors as her daughter struggled with her health, before she solved the medical mystery on her own.<\/p>\n<p>Austin Carrigg&#8217;s daughter, Melanie, wasn&#8217;t reaching developmental milestones like other children with Down syndrome. She never learned to hold her head up or sit on her own, both things that children with Down syndrome are expected to do. Yet doctors told Carrigg the reason was simply because of Melanie&#8217;s Down syndrome.<\/p>\n<p>\u201cI remember taking her to a developmental pediatrician and saying, \u2018I know something is very wrong and we\u2019re here to see you because you\u2019re the type of doctor who helps us figure out why she\u2019s not meeting her milestones,\u2019\u201d Carrigg <a href=\"https:\/\/www.today.com\/today\/amp\/tdna227242\" target=\"_blank\" rel=\"noopener\">told TODAY<\/a>. \u201cHe said to me, \u2018She\u2019s never going to walk. She\u2019s never going to talk. I never need to see you again.\u2019\u201d<\/p>\n<p><strong>READ:\u00a0<em><a href=\"https:\/\/archive.liveaction.org\/news\/mother-daughter-business-owners-down-syndrome-dream\/\">Mother-daughter business owners show others with Down syndrome that no dream is too big<\/a><\/em><\/strong><\/p>\n<p>Yet Carrigg knew something else was wrong, especially as Melanie&#8217;s condition worsened \u2014 she slept all day, and then started getting sick. \u201cShe had thrown up once and then we couldn\u2019t wake her,\u201d she said. \u201cWhen we could rouse her she would fight us. She was hitting and, like, pulling away. So we rushed to the ER.&#8221;<\/p>\n<p>Things were so bad that Melanie was in a coma, brought on by low blood sugar and high ketones. When they got home, Carrigg continued to look for answers, and finally received a referral to a metabolic geneticist. There, she got the answers she&#8217;d been desperately searching for: Melanie had ketotic hypoglycemia, a medical condition that causes low blood sugar and ketosis.<\/p>\n<p style=\"text-align: center;\"><iframe loading=\"lazy\" style=\"border: none; overflow: hidden;\" src=\"https:\/\/www.facebook.com\/plugins\/video.php?height=314&amp;href=https%3A%2F%2Fwww.facebook.com%2Fketotichypoglycemiainternational%2Fvideos%2F1061983184258655%2F&amp;show_text=true&amp;width=560&amp;t=0\" width=\"560\" height=\"429\" frameborder=\"0\" scrolling=\"no\" allowfullscreen=\"allowfullscreen\"><\/iframe>\n<\/p>\n<p>\u201cIt was a relief,\u201d she said. \u201cThe world was spinning because it felt so surreal. I finally know I\u2019m not crazy. They\u2019re finally going to help me help her.\u201d<\/p>\n<p>And the treatment was incredibly easy. \u201cYou take cornstarch,\u201d Carrigg explained. \u201cBelieve it or not, that simple thing,\u00a0cornstarch, maintains blood sugar. Within six months of being put on cornstarch she was walking. Our kiddo who would sleep all day every day, didn\u2019t sleep all day every day. She was awake and she was thriving and playing.\u201d<\/p>\n<p>Soon, Melanie began meeting her milestones, too. But Carrigg wasn&#8217;t done fighting. She had noticed something when talking to other parents of children with Down syndrome: many of their children had ketotic hypoglycemia, too. \u201cI just thought to myself, \u2018What are the odds that this other little girl with Down syndrome, also has a blood sugar issue that my daughter does?\u2019\u201d she said. \u201cI realized there had to be something there.\u201d<\/p>\n<p>Sh reached out to Ketotic Hypoglycemia International, whose executive director, Danielle Drachmann, put her in touch with their advisory board \u2014 and they took her seriously. They launched a <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/jmd2.12241\" target=\"_blank\" rel=\"noopener\">research survey<\/a> of parents of children with Down syndrome, graciously including Carrigg as an author, and found that 7% of respondents either had a diagnosis of ketotic hypoglycemia, or symptoms consistent with it.<\/p>\n<p>It was the first time a connection between Down syndrome and ketotic hypoglycemia had been found, which was both exciting and disappointing.<\/p>\n<p>&#8220;We hoped not to see that Down syndrome patients had been overlooked for their low blood sugar. It is easy to diagnose once you have the suspicion,\u201d Dr. Henrik Thybo Christesen, one of the authors of the paper, told TODAY.<\/p>\n<p>Co-author Jacob Sten Petersen added, \u201cSince Down syndrome is such a complicated genetic disease with many different manifestations, some of which may resemble low blood glucose, this is probably why in the past (ketotic hypoglycemia has) been completely overlooked.&#8221;<\/p>\n<p>And it all came from their willingness to listen to a mom&#8217;s gut instinct, when other doctors refused. \u201cThey gave me my voice,\u201d she said. \u201cI\u2019m her mom. I know her best&#8230; There\u2019s this other team of doctors who valued my opinion and I was right.\u201d<\/p>\n<p style=\"text-align: center;\"><strong><em><a href=\"https:\/\/www.facebook.com\/liveactionnewsonline\/?ref=br_rs\" target=\"_blank\" rel=\"noopener\">\u201cLike\u201d Live Action News on Facebook<\/a>\u00a0for more pro-life news and commentary!<\/em><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A mom of a child with Down syndrome says she was repeatedly ignored by doctors as her daughter struggled with her health, before she solved the medical mystery on her own. Austin Carrigg&#8217;s daughter, Melanie, wasn&#8217;t reaching developmental milestones like other children with Down syndrome. She never learned to hold her head up or sit [&hellip;]<\/p>\n","protected":false},"author":7,"featured_media":250799,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[9455,3473],"tags":[11719,429,11715,11720,11721,11718,11716,11717],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Determined mom makes medical breakthrough for children with Down syndrome<\/title>\n<meta name=\"description\" content=\"When doctors blamed her daughter&#039;s puzzling symptoms on her Down syndrome, mom Austin Carrigg didn&#039;t give up, and finally found the real answer.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/determined-mom-medical-breakthrough-down-syndrome\/\" 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